A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986785



Internal ID12979566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40369961..40435361hg38UCSC Ensembl
Innerchr7:40409560..40474960hg19UCSC Ensembl
Innerchr7:40376085..40441485hg18UCSC Ensembl
Innerchr7:40182800..40248200hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3865401
hg1965401
hg1865401
hg1765401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34484
Supporting Variants
SamplesNA12872
Known GenesC7orf10
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986785
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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